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Microetcher

by Danville Engineering, Inc. 510(k)

Active United States

510(k) K902836

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK902836 Date20 Nov 1990ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
KOJ
Device Class
Class II
Regulation
21 CFR Part 872.6080
Advisory Committee
Dental
FDA Decision
SESE Substantially Equivalent

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